Bupropion (xl recalls
The FDA has published 3 recalls involving Bupropion (xl since 2012. The latest was reported on 22 Jan 2014. Most were for potency & assay. McKesson Packaging Services has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls3since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 22 Jan 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 33%Class III 2 67%
Why bupropion (xl is recalled
Companies
By year
All bupropion (xl recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | buPROPion HCl ER (XL), Tablet, 150 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS III | buPROPion Hydrochloride Extended-Release Tablets (XL) recalled | McKesson Packaging Services | Potency & Assay | Nationwide |
| Drug | CLASS III | buPROPion Hydrochloride Extended-Release Tablets (XL) recalled | McKesson Packaging Services | Potency & Assay | Nationwide |
Should you stop taking Bupropion (xl?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.